ES2240800T3 - Formulaciones de plaguicidas que contienen ciertos copolimeros. - Google Patents

Formulaciones de plaguicidas que contienen ciertos copolimeros.

Info

Publication number: ES2240800T3
Authority: ES; Spain
Prior art keywords: acid; pesticide formulations; formulations according; component; case
Prior art date: 2001-04-10
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired - Lifetime

Application number

ES02769122T

Other languages

English (en)

Spanish (es)

Inventor

Ralf Zerrer

Gerd Roland Meyer

Franz Xaver Scherl

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Clariant Produkte Deutschland GmbH

Original Assignee

Clariant GmbH

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2001-04-10

Filing date

2002-04-06

Publication date

2005-10-16

2002-04-06 Application filed by Clariant GmbH filed Critical Clariant GmbH

2005-10-16 Application granted granted Critical

2005-10-16 Publication of ES2240800T3 publication Critical patent/ES2240800T3/es

2022-04-06 Anticipated expiration legal-status Critical

Status Expired - Lifetime legal-status Critical Current

Links

229920001577 copolymer Polymers 0.000 title claims abstract description 51
239000000203 mixture Substances 0.000 title claims description 33
239000000575 pesticide Substances 0.000 title claims description 24
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims abstract description 58
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims abstract description 31
239000003090 pesticide formulation Substances 0.000 claims abstract description 30
150000002762 monocarboxylic acid derivatives Chemical class 0.000 claims abstract description 18
238000007334 copolymerization reaction Methods 0.000 claims abstract description 12
125000000217 alkyl group Chemical group 0.000 claims abstract description 8
125000003342 alkenyl group Chemical group 0.000 claims abstract description 7
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 6
125000001624 naphthyl group Chemical group 0.000 claims abstract description 3
239000002253 acid Substances 0.000 claims description 38
229920000223 polyglycerol Polymers 0.000 claims description 29
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims description 22
XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical group OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims description 17
239000004009 herbicide Substances 0.000 claims description 17
239000005562 Glyphosate Substances 0.000 claims description 14
229940097068 glyphosate Drugs 0.000 claims description 14
235000013162 Cocos nucifera Nutrition 0.000 claims description 12
244000060011 Cocos nucifera Species 0.000 claims description 12
235000014113 dietary fatty acids Nutrition 0.000 claims description 11
239000000194 fatty acid Substances 0.000 claims description 11
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150000004665 fatty acids Chemical class 0.000 claims description 11
230000004071 biological effect Effects 0.000 claims description 9
MUBZPKHOEPUJKR-UHFFFAOYSA-N oxalic acid group Chemical group C(C(=O)O)(=O)O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 9
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 8
150000001991 dicarboxylic acids Chemical class 0.000 claims description 8
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 8
238000000034 method Methods 0.000 claims description 7
150000003839 salts Chemical class 0.000 claims description 7
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 4
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 4
239000000417 fungicide Substances 0.000 claims description 4
239000008187 granular material Substances 0.000 claims description 4
239000002917 insecticide Substances 0.000 claims description 4
WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 claims description 4
239000003760 tallow Substances 0.000 claims description 4
125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 3
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RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 claims description 2
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 2
239000001361 adipic acid Substances 0.000 claims description 2
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JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 claims description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 claims description 2
239000000843 powder Substances 0.000 claims description 2
239000003826 tablet Substances 0.000 claims description 2
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims 2
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125000000129 anionic group Chemical group 0.000 description 5
238000004132 cross linking Methods 0.000 description 5
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IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
238000013019 agitation Methods 0.000 description 4
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239000003995 emulsifying agent Substances 0.000 description 4
150000002763 monocarboxylic acids Chemical class 0.000 description 4
238000006116 polymerization reaction Methods 0.000 description 4
230000009471 action Effects 0.000 description 3
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238000006243 chemical reaction Methods 0.000 description 3
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239000012467 final product Substances 0.000 description 3
IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 3
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FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 2
240000005702 Galium aparine Species 0.000 description 2
235000014820 Galium aparine Nutrition 0.000 description 2
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235000011999 Panicum crusgalli Nutrition 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
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150000007513 acids Chemical class 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
229910052783 alkali metal Inorganic materials 0.000 description 2
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150000003973 alkyl amines Chemical class 0.000 description 2
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HAMNKKUPIHEESI-UHFFFAOYSA-N aminoguanidine Chemical compound NNC(N)=N HAMNKKUPIHEESI-UHFFFAOYSA-N 0.000 description 2
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239000007864 aqueous solution Substances 0.000 description 2
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239000011230 binding agent Substances 0.000 description 2
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239000001913 cellulose Substances 0.000 description 2
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239000003085 diluting agent Substances 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
210000002615 epidermis Anatomy 0.000 description 2
235000019197 fats Nutrition 0.000 description 2
KEMQGTRYUADPNZ-UHFFFAOYSA-N heptadecanoic acid Chemical compound CCCCCCCCCCCCCCCCC(O)=O KEMQGTRYUADPNZ-UHFFFAOYSA-N 0.000 description 2
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VKOBVWXKNCXXDE-UHFFFAOYSA-N icosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCC(O)=O VKOBVWXKNCXXDE-UHFFFAOYSA-N 0.000 description 2
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QYPPRTNMGCREIM-UHFFFAOYSA-N methylarsonic acid Chemical compound C[As](O)(O)=O QYPPRTNMGCREIM-UHFFFAOYSA-N 0.000 description 2
WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 2
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ISYWECDDZWTKFF-UHFFFAOYSA-N nonadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCCC(O)=O ISYWECDDZWTKFF-UHFFFAOYSA-N 0.000 description 2
239000003921 oil Substances 0.000 description 2
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239000000600 sorbitol Substances 0.000 description 2
SZHOJFHSIKHZHA-UHFFFAOYSA-N tridecanoic acid Chemical compound CCCCCCCCCCCCC(O)=O SZHOJFHSIKHZHA-UHFFFAOYSA-N 0.000 description 2
238000009736 wetting Methods 0.000 description 2
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JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
125000006526 (C1-C2) alkyl group Chemical group 0.000 description 1
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
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235000020661 alpha-linolenic acid Nutrition 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
CEGOLXSVJUTHNZ-UHFFFAOYSA-K aluminium tristearate Chemical compound [Al+3].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CEGOLXSVJUTHNZ-UHFFFAOYSA-K 0.000 description 1
229940063655 aluminum stearate Drugs 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
150000001413 amino acids Chemical class 0.000 description 1
150000003863 ammonium salts Chemical class 0.000 description 1
BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
150000008064 anhydrides Chemical class 0.000 description 1
239000010775 animal oil Substances 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
235000010323 ascorbic acid Nutrition 0.000 description 1
229960005070 ascorbic acid Drugs 0.000 description 1
239000011668 ascorbic acid Substances 0.000 description 1
235000010385 ascorbyl palmitate Nutrition 0.000 description 1
VGPYEHKOIGNJKV-UHFFFAOYSA-N asulam Chemical compound COC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 VGPYEHKOIGNJKV-UHFFFAOYSA-N 0.000 description 1
208000014347 autosomal dominant hyaline body myopathy Diseases 0.000 description 1
OTSAMNSACVKIOJ-UHFFFAOYSA-N azane;carbamoyl(ethoxy)phosphinic acid Chemical compound [NH4+].CCOP([O-])(=O)C(N)=O OTSAMNSACVKIOJ-UHFFFAOYSA-N 0.000 description 1
229940116226 behenic acid Drugs 0.000 description 1
HYJSGOXICXYZGS-UHFFFAOYSA-N benazolin Chemical compound C1=CC=C2SC(=O)N(CC(=O)O)C2=C1Cl HYJSGOXICXYZGS-UHFFFAOYSA-N 0.000 description 1
230000008901 benefit Effects 0.000 description 1
ZOMSMJKLGFBRBS-UHFFFAOYSA-N bentazone Chemical compound C1=CC=C2NS(=O)(=O)N(C(C)C)C(=O)C2=C1 ZOMSMJKLGFBRBS-UHFFFAOYSA-N 0.000 description 1
CNBGNNVCVSKAQZ-UHFFFAOYSA-N benzidamine Natural products C12=CC=CC=C2C(OCCCN(C)C)=NN1CC1=CC=CC=C1 CNBGNNVCVSKAQZ-UHFFFAOYSA-N 0.000 description 1
DMSMPAJRVJJAGA-UHFFFAOYSA-N benzo[d]isothiazol-3-one Chemical compound C1=CC=C2C(=O)NSC2=C1 DMSMPAJRVJJAGA-UHFFFAOYSA-N 0.000 description 1
235000010233 benzoic acid Nutrition 0.000 description 1
GINJFDRNADDBIN-FXQIFTODSA-N bilanafos Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@@H](N)CCP(C)(O)=O GINJFDRNADDBIN-FXQIFTODSA-N 0.000 description 1
229910021538 borax Inorganic materials 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000006229 carbon black Substances 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
QZXCCPZJCKEPSA-UHFFFAOYSA-N chlorfenac Chemical compound OC(=O)CC1=C(Cl)C=CC(Cl)=C1Cl QZXCCPZJCKEPSA-UHFFFAOYSA-N 0.000 description 1
229930002875 chlorophyll Natural products 0.000 description 1
235000019804 chlorophyll Nutrition 0.000 description 1
ATNHDLDRLWWWCB-AENOIHSZSA-M chlorophyll a Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 ATNHDLDRLWWWCB-AENOIHSZSA-M 0.000 description 1
238000001246 colloidal dispersion Methods 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 description 1
ZPWVASYFFYYZEW-UHFFFAOYSA-L dipotassium hydrogen phosphate Chemical compound [K+].[K+].OP([O-])([O-])=O ZPWVASYFFYYZEW-UHFFFAOYSA-L 0.000 description 1
235000019797 dipotassium phosphate Nutrition 0.000 description 1
229910000396 dipotassium phosphate Inorganic materials 0.000 description 1
UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 description 1
238000004945 emulsification Methods 0.000 description 1
230000032050 esterification Effects 0.000 description 1
238000005886 esterification reaction Methods 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
238000000605 extraction Methods 0.000 description 1
BGZZWXTVIYUUEY-UHFFFAOYSA-N fomesafen Chemical compound C1=C([N+]([O-])=O)C(C(=O)NS(=O)(=O)C)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 BGZZWXTVIYUUEY-UHFFFAOYSA-N 0.000 description 1
230000008014 freezing Effects 0.000 description 1
238000007710 freezing Methods 0.000 description 1
230000012010 growth Effects 0.000 description 1
229940093915 gynecological organic acid Drugs 0.000 description 1
235000008216 herbs Nutrition 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
238000009413 insulation Methods 0.000 description 1
239000013067 intermediate product Substances 0.000 description 1
NRXQIUSYPAHGNM-UHFFFAOYSA-N ioxynil Chemical compound OC1=C(I)C=C(C#N)C=C1I NRXQIUSYPAHGNM-UHFFFAOYSA-N 0.000 description 1
YAQXGBBDJYBXKL-UHFFFAOYSA-N iron(2+);1,10-phenanthroline;dicyanide Chemical compound [Fe+2].N#[C-].N#[C-].C1=CN=C2C3=NC=CC=C3C=CC2=C1.C1=CN=C2C3=NC=CC=C3C=CC2=C1 YAQXGBBDJYBXKL-UHFFFAOYSA-N 0.000 description 1
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
229960004488 linolenic acid Drugs 0.000 description 1
KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
238000005259 measurement Methods 0.000 description 1
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
235000010270 methyl p-hydroxybenzoate Nutrition 0.000 description 1
229960002939 metizoline Drugs 0.000 description 1
239000011707 mineral Substances 0.000 description 1
238000002156 mixing Methods 0.000 description 1
JITOKQVGRJSHHA-UHFFFAOYSA-M monosodium methyl arsenate Chemical compound [Na+].C[As](O)([O-])=O JITOKQVGRJSHHA-UHFFFAOYSA-M 0.000 description 1
JXTHEWSKYLZVJC-UHFFFAOYSA-N naptalam Chemical compound OC(=O)C1=CC=CC=C1C(=O)NC1=CC=CC2=CC=CC=C12 JXTHEWSKYLZVJC-UHFFFAOYSA-N 0.000 description 1
239000005445 natural material Substances 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
229940098695 palmitic acid Drugs 0.000 description 1
230000003071 parasitic effect Effects 0.000 description 1
230000000361 pesticidal effect Effects 0.000 description 1
230000029553 photosynthesis Effects 0.000 description 1
238000010672 photosynthesis Methods 0.000 description 1
NQQVFXUMIDALNH-UHFFFAOYSA-N picloram Chemical compound NC1=C(Cl)C(Cl)=NC(C(O)=O)=C1Cl NQQVFXUMIDALNH-UHFFFAOYSA-N 0.000 description 1
230000008654 plant damage Effects 0.000 description 1
230000008635 plant growth Effects 0.000 description 1
229920000768 polyamine Polymers 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
229920001282 polysaccharide Polymers 0.000 description 1
239000005017 polysaccharide Substances 0.000 description 1
229920005591 polysilicon Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
230000008569 process Effects 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical class CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 1
239000003223 protective agent Substances 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
239000003128 rodenticide Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
235000003441 saturated fatty acids Nutrition 0.000 description 1
150000004671 saturated fatty acids Chemical class 0.000 description 1
238000000926 separation method Methods 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
229910052710 silicon Inorganic materials 0.000 description 1
239000010703 silicon Substances 0.000 description 1
239000001632 sodium acetate Substances 0.000 description 1
235000017281 sodium acetate Nutrition 0.000 description 1
WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
235000010234 sodium benzoate Nutrition 0.000 description 1
239000004299 sodium benzoate Substances 0.000 description 1
235000019351 sodium silicates Nutrition 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
235000010339 sodium tetraborate Nutrition 0.000 description 1
239000004328 sodium tetraborate Substances 0.000 description 1
235000019832 sodium triphosphate Nutrition 0.000 description 1
239000000243 solution Substances 0.000 description 1
229940075554 sorbate Drugs 0.000 description 1
238000001179 sorption measurement Methods 0.000 description 1
238000005507 spraying Methods 0.000 description 1
230000007480 spreading Effects 0.000 description 1
238000003892 spreading Methods 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
238000003860 storage Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
239000001384 succinic acid Substances 0.000 description 1
239000005720 sucrose Substances 0.000 description 1
235000000346 sugar Nutrition 0.000 description 1
150000008163 sugars Chemical class 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
210000001519 tissue Anatomy 0.000 description 1
235000021122 unsaturated fatty acids Nutrition 0.000 description 1
150000004670 unsaturated fatty acids Chemical class 0.000 description 1
229920001285 xanthan gum Polymers 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/30—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests characterised by the surfactants
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals

Landscapes

Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Health & Medical Sciences (AREA)
Dentistry (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Agronomy & Crop Science (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Toxicology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Polyesters Or Polycarbonates (AREA)
Confectionery (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

ES02769122T 2001-04-10 2002-04-06 Formulaciones de plaguicidas que contienen ciertos copolimeros. Expired - Lifetime ES2240800T3 (es)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE10117993A DE10117993A1 (de)	2001-04-10	2001-04-10	Pestizidzubereitungen enthaltend Copolymere
DE10117993		2001-04-10

Publications (1)

Publication Number	Publication Date
ES2240800T3 true ES2240800T3 (es)	2005-10-16

Family

ID=7681165

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ES02769122T Expired - Lifetime ES2240800T3 (es)	2001-04-10	2002-04-06	Formulaciones de plaguicidas que contienen ciertos copolimeros.

Country Status (15)

Country	Link
US (1)	US7407667B2 (de)
EP (1)	EP1379129B1 (de)
JP (1)	JP4298298B2 (de)
KR (1)	KR100862876B1 (de)
CN (1)	CN1250077C (de)
AT (1)	ATE292381T1 (de)
BR (1)	BR0208737B1 (de)
CA (1)	CA2443817C (de)
DE (2)	DE10117993A1 (de)
DK (1)	DK1379129T3 (de)
ES (1)	ES2240800T3 (de)
IL (2)	IL158290A0 (de)
MX (1)	MXPA03009183A (de)
MY (1)	MY129826A (de)
WO (1)	WO2002089575A1 (de)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE10130357A1 (de) *	2001-06-23	2003-01-02	Clariant Gmbh	Pestizidzubereitungen enthaltend Copolymere
DE10211801B4 (de) *	2002-03-16	2004-09-30	Clariant Gmbh	Kosmetische und pharmazeutische Zubereitungen enthaltend einen oxalkylierten Polyglycerinester
DE10307171B4 (de) *	2003-02-20	2009-04-16	Clariant Produkte (Deutschland) Gmbh	Copolymere enthaltende landwirschaftliche Mittel
DE10342870A1 (de)	2003-09-15	2005-05-12	Clariant Gmbh	Flüssige Zusammensetzungen enthaltend oxalkylierte Polyglycerinester
GB0423072D0 (en)	2004-10-18	2004-11-17	Ici Plc	Surfactant compounds
EP1905302A1 (de) *	2006-09-30	2008-04-02	Bayer CropScience AG	Suspensionskonzentrate
NZ552290A (en) *	2006-12-21	2009-05-31	Bomac Research Ltd	Tablet fomulation
US7655597B1 (en)	2009-08-03	2010-02-02	Specialty Fertilizer Products, Llc	Pesticide compositions including polymeric adjuvants
DE102009041003A1 (de)	2009-09-10	2011-03-24	Clariant International Limited	Pestizidzubereitungen
GB201011852D0 (en)	2010-07-14	2010-09-01	Croda Int Plc	Novel oligoester
DE102011013556A1 (de)	2011-03-10	2012-09-13	Clariant International Ltd.	Zusammensetzungen enthaltend Copolymere
DE102011014354A1 (de) *	2011-03-17	2012-09-20	Clariant International Ltd.	Suspensionskonzentrate
US9826734B2 (en)	2011-07-26	2017-11-28	Clariant International Ltd.	Etherified lactate esters, method for the production thereof and use thereof for enhancing the effect of plant protecting agents
DE102012002272A1 (de)	2012-02-04	2013-08-08	Clariant International Ltd.	Pestizid-Zusammensetzungen
CN104640965A (zh)	2012-05-30	2015-05-20	科莱恩金融(Bvi)有限公司	包含n-甲基-n-酰基葡糖胺的组合物
EP2854751B1 (de)	2012-05-30	2016-08-10	Clariant International Ltd.	Verwendung von n-methyl-n-acylglucaminen als solubilisatoren
BR112015008776B1 (pt) *	2012-10-24	2021-05-04	Clariant International Ltd	uso de copolímeros e método para reduzir deriva na aplicação de formulações pesticidas
DE102012021647A1 (de) *	2012-11-03	2014-05-08	Clariant International Ltd.	Wässrige Adjuvant-Zusammensetzungen
DE102014005771A1 (de) *	2014-04-23	2015-10-29	Clariant International Ltd.	Verwendung von wässrigen driftreduzierenden Zusammensetzungen
DE202014008417U1 (de)	2014-04-30	2014-11-24	Clariant International Ltd.	Tensidkonzentrate zur Förderung von Bodenbefeuchtung und Pflanzenwachstum
DE102014012022A1 (de) *	2014-08-13	2016-02-18	Clariant International Ltd.	Organische Ammoniumsalze von anionischen Pestiziden
DE102015213635A1 (de)	2015-07-20	2017-01-26	Clariant International Ltd	Pflanzennährstoff-Suspensionen und deren Verwendung zum Düngen von Pflanzen
DE102015219651A1 (de)	2015-10-09	2017-04-13	Clariant International Ltd.	Zusammensetzungen enthaltend Zuckeramin und Fettsäure
DE202015008045U1 (de)	2015-10-09	2015-12-09	Clariant International Ltd.	Universelle Pigmentdispersionen auf Basis von N-Alkylglukaminen
DE102016207877A1 (de)	2016-05-09	2017-11-09	Clariant International Ltd	Stabilisatoren für Silikatfarben
EP3893846B1 (de)	2018-12-11	2024-12-04	Dow Global Technologies LLC	Wässrige lösungen schwerlöslicher wirkstoffe unter verwendung von polyalkoxylierten aminoalkoholen
JP7465267B2 (ja)	2018-12-11	2024-04-10	ダウグローバルテクノロジーズエルエルシー	ポリアルコキシル化アルコールを使用する難溶性農薬の水溶液

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NL235788A (de) *	1958-02-13
US3816092A (en)	1958-02-13	1974-06-11	Rohm & Haas	Herbicidal 3,1-dichloroanilides
DE3417646A1 (de)	1984-05-12	1985-11-14	Henkel Kgaa	Haarnachbehandlungsmittel
DE3614788A1 (de) *	1986-05-02	1987-11-05	Hoechst Ag	Herbizide emulsionen
KR920700544A (ko)	1988-12-27	1992-08-10	아놀드 하비 콜	극성 및 비극성 제초제를 함유한 조성물
JPH0397789A (ja) *	1989-09-11	1991-04-23	Nippon Steel Corp	レールおよび車輪用潤滑剤
JP3228571B2 (ja) *	1991-10-31	2001-11-12	花王株式会社	農薬用効力増強剤及び農薬組成物
EP0577914A1 (de)	1992-07-08	1994-01-12	Monsanto Europe S.A./N.V.	Verbesserte Glyphosat-Zusammensetzungen und ihre Verwendung
US5750468A (en) *	1995-04-10	1998-05-12	Monsanto Company	Glyphosate formulations containing etheramine surfactants
US5710103A (en) *	1996-04-03	1998-01-20	Albemarle Corporation	Glyphosate compositions comprising hydrocarbyl dimethyl amine oxide and quaternary ammonium halide
ATE252827T1 (de)	1996-08-16	2003-11-15	Monsanto Technology Llc	Reihenanordnungsmethode zur behandlung von pflanzen mit exogenen chemikalien
AU746589B2 (en)	1997-07-30	2002-05-02	Monsanto Company	Process and compositions promoting biological effectiveness of exogenous chemical substances in plants
WO2001008481A1 (de) *	1999-07-30	2001-02-08	Clariant Gmbh	Pestizidzubereitungen enthaltend polyglycerine oder polyglycerinderivate

2001
- 2001-04-10 DE DE10117993A patent/DE10117993A1/de not_active Withdrawn
2002
- 2002-04-06 DK DK02769122T patent/DK1379129T3/da active
- 2002-04-06 WO PCT/EP2002/003827 patent/WO2002089575A1/de not_active Ceased
- 2002-04-06 EP EP02769122A patent/EP1379129B1/de not_active Expired - Lifetime
- 2002-04-06 CA CA002443817A patent/CA2443817C/en not_active Expired - Lifetime
- 2002-04-06 JP JP2002586728A patent/JP4298298B2/ja not_active Expired - Lifetime
- 2002-04-06 KR KR1020037013249A patent/KR100862876B1/ko not_active Expired - Fee Related
- 2002-04-06 BR BRPI0208737-5A patent/BR0208737B1/pt active IP Right Grant
- 2002-04-06 AT AT02769122T patent/ATE292381T1/de active
- 2002-04-06 US US10/474,559 patent/US7407667B2/en not_active Expired - Lifetime
- 2002-04-06 MX MXPA03009183A patent/MXPA03009183A/es active IP Right Grant
- 2002-04-06 CN CNB028079957A patent/CN1250077C/zh not_active Expired - Lifetime
- 2002-04-06 ES ES02769122T patent/ES2240800T3/es not_active Expired - Lifetime
- 2002-04-06 DE DE50202717T patent/DE50202717D1/de not_active Expired - Lifetime
- 2002-04-06 IL IL15829002A patent/IL158290A0/xx active IP Right Grant
- 2002-04-09 MY MYPI20021266A patent/MY129826A/en unknown
2003
- 2003-10-07 IL IL158290A patent/IL158290A/en unknown

Also Published As

Publication number	Publication date
CA2443817C (en)	2008-09-16
JP4298298B2 (ja)	2009-07-15
KR20030088495A (ko)	2003-11-19
DE50202717D1 (de)	2005-05-12
CN1501772A (zh)	2004-06-02
JP2004525189A (ja)	2004-08-19
IL158290A (en)	2007-05-15
BR0208737A (pt)	2004-07-20
MY129826A (en)	2007-05-31
EP1379129B1 (de)	2005-04-06
CN1250077C (zh)	2006-04-12
EP1379129A1 (de)	2004-01-14
MXPA03009183A (es)	2004-02-17
US7407667B2 (en)	2008-08-05
IL158290A0 (en)	2004-05-12
KR100862876B1 (ko)	2008-10-15
HK1065220A1 (en)	2005-02-18
ATE292381T1 (de)	2005-04-15
DK1379129T3 (da)	2005-06-20
BR0208737B1 (pt)	2013-04-30
US20060166826A1 (en)	2006-07-27
WO2002089575A1 (de)	2002-11-14
CA2443817A1 (en)	2002-11-14
DE10117993A1 (de)	2002-10-17

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US7407667B2 (en)	2008-08-05	Pesticidal preparations comprising copolymers
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US11425904B2 (en)	2022-08-30	Use of aqueous drift-reducing compositions
CN106386848A (zh)	2017-02-15	包含草甘膦和烷氧基化甘油酯的除草配制剂
NZ502499A (en)	2001-11-30	Herbicide consisting of glyphosate composition and polyamine derivatives
AU2012299858B2 (en)	2015-10-01	Pesticide preparations
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CA2516694A1 (en)	2004-09-02	Agricultural agents containing copolymers
DE19936092A1 (de)	2001-02-01	Polyglycerinester enthaltende Pestizidzubereitungen
HK1087593B (en)	2008-07-25	Agricultural agents containing copolymers
HK1065220B (en)	2006-11-10	Pesticidal preparations comprising copolymers
KR20050103235A (ko)	2005-10-27	공중합체를 함유하는 농약 제제
HK1066702B (en)	2006-10-13	Pesticide preparations containing copolymers